首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Study on X-ray-induced apoptosis and chromosomal damage in G2 human lymphocytes in the presence of pifithrin-alpha, an inhibitor of p53.
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Study on X-ray-induced apoptosis and chromosomal damage in G2 human lymphocytes in the presence of pifithrin-alpha, an inhibitor of p53.

机译:在p53抑制剂pifithrin-α存在下,X射线诱导的G2人淋巴细胞凋亡和染色体损伤的研究。

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The aim of this study is to investigate the role of the cell-cycle phase in cells exposed to radiation and chemicals in relation to the cellular response. The analysis was focused on the G2 cell-cycle phase, exploring the impact of p53 inhibition in human lymphocytes irradiated with X-rays in the presence or absence of pifithrin-alpha (PFT-alpha), a p53-specific inhibitor. Lymphocytes, 44h after stimulation to proliferate, were X-irradiated with 0.5Gy both in the presence or the absence of PFT-alpha and post-treated with a pulse of 5-bromodeoxyuridine (BrdUrd) to distinguish cells in the S- or G2-phase at the moment of irradiation. At early sampling times after X-ray exposure the following parameters were analysed: cellular proliferation, apoptosis, chromosomal aberrations and p53 expression. The results show an enhancement of apoptotic cells in G2 at early sampling times after irradiation and no differences in terms of chromosomal aberration induction both in cells treated with X-rays alone and in cells treated with X-rays plus PFT-alpha. Expression of p53 was not detectable at all recovery times. The results suggest a p53-independent apoptotic pathway acting at early times after X-ray exposure in G2 lymphocytes. Furthermore, the same yield of X-ray-induced chromatid breaks was observed both in the presence or absence of PFT-alpha implying that in G2 X-irradiated lymphocytes this inhibitor of the p53 protein does not affect DNA repair.
机译:这项研究的目的是研究细胞周期相在暴露于辐射和化学物质的细胞中与细胞反应有关的作用。该分析集中在G2细胞周期阶段,探讨了在存在或不存在p53特异性抑制剂pifithrin-alpha(PFT-alpha)的情况下,p53抑制作用在用X射线照射的人淋巴细胞中的影响。在存在或不存在PFT-α的情况下,将刺激增殖后44h的淋巴细胞进行0.5Gy的X射线照射,然后用5-溴脱氧尿苷(BrdUrd)脉冲进行后处理,以区分S-或G2-细胞照射时的相位。 X射线暴露后的早期采样时间分析以下参数:细胞增殖,凋亡,染色体畸变和p53表达。结果表明,在照射后的早期采样时间,G2中的凋亡细胞增强,并且在单独使用X射线处理的细胞和使用X射线加PFT-alpha处理的细胞中,在染色体畸变诱导方面均无差异。在所有恢复时间均未检测到p53的表达。结果表明,在X射线暴露于G2淋巴细胞后的早期,有一个独立于p53的凋亡途径。此外,在存在或不存在PFT-α的情况下,观察到X射线诱导的染色单体断裂的收率相同,这表明在G2 X射线照射的淋巴细胞中,p53蛋白的这种抑制剂不会影响DNA修复。

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